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Up to: Autoimmune disease · Pulmonary alveolar proteinosis

Autoimmune pulmonary alveolar proteinosis

Pulmonary alveolar proteinosis (PAP) is a rare lung disease characterized by the accumulation of a lipoproteinaceous substance in the distal air spaces which positively stains with periodic acid-Schiff (PAS).

6 trials tagged with this condition →

This condition has no sub-types.